A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9813



Internal ID15193189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1886312..1922452hg38UCSC Ensembl
Outerchr11:1907542..1943682hg19UCSC Ensembl
Outerchr11:1864118..1900258hg18UCSC Ensembl
Outerchr11:1864118..1900258hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3836141
hg1936141
hg1836141
hg1736141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7213
Supporting Variants
SamplesNA18507
Known GenesLSP1, TNNT3
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9813
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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